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Food and Drug Administrations timetable for requiring Substantial Equivalence (SE) applications has been the topic of discussion among many manufacturers for the past few weeks

Youre not going to learn much by comparing vapes based on their puff counts, though, because manufacturers have different methods of determining how many puffs their devices should deliver

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Opposition from anti-tobacco organizations, health and medical associations, and, in particular, a quartet of federal entitiesthe surgeon general, the Centers for Disease Control and Prevention, the National Institutes of Health, and the Food and Drug Administration (FDA)has slowed transition, left consumers disorientated, protected the cigarette trade, and damaged or destroyed hundreds of pro-health businesses